Evidence map›Paper›PMID 40682121›Full record

ArticleG3 (Bethesda, Md.)2025

Family-based selection: an efficient method for increasing phenotypic variability.

Shraddha Lall, Chris Milton, Benjamin de Bivort

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Shraddha LallDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138, United States.ORCID 0000-0001-7654-8003
Chris MiltonDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138, United States.
Benjamin de BivortDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138, United States.ORCID 0000-0001-6165-7696

Funding

Structural Variation in Neuronal Circuits as a Basis for Functional and Behavioral IndividualityR01NS121874 · NINDS · HARVARD MEDICAL SCHOOL · PI DE BIVORT, BENJAMIN, HASSAN, BASSEM A · 2021 to 2025
$5.0M
NIHNINDS NIH HHS 1R01NS121874-01NINDS NIH HHS R01 NS121874
6 · The paper itself

Abstract

Persistent idiosyncrasies in behavioral phenotypes have been documented across animal taxa. These individual differences among organisms from the same genotype and reared in identical environments can result in phenotypic variability in the absence of genetic variation. While there is strong evidence to suggest that variability of traits can be heritable and determined by the genotype of an organism, little is known about how selection can specifically shape this heritable variance. Here, we describe a Python-based model of directional artificial selection for increasing the variability of a polygenic trait of interest. Specifically, our model focuses on variability in left-vs-right turn bias in Drosophila melanogaster. While the mean value of turn bias for a genotype is non-heritable and constant across genotypes, the variability of turn bias is a heritable and polygenic trait, varying dramatically among different genetic lines. Using our model, we compare different selection regimes and predict selection dynamics at population and genetic levels. We find that introducing population structure via a family-based selection regime can significantly affect selection response. When selection for increased variability is implemented on the basis of independently measured traits of individuals, the response is slower, but leads to a population with a greater genetic diversity. In contrast, when selection is implemented by measuring traits of families with half or full siblings, the response is faster, albeit with a reduced final genetic diversity in the population. Our model provides a useful starting point to study the effect of different selection regimes on any polygenic trait of interest. We can use this model to predict responses of laboratory-based selection experiments and implement feasible experiments for selection of complex polygenic traits in the laboratory.

Indexed as

Models, GeneticPhenotypeSelection, GeneticAnimalsDrosophila melanogasterGenetic VariationGenotypeMultifactorial Inheritanceartificial selectionbehavioral individualityfamily-based selection; Drosophila melanogastermodelingphenotypic variability

Identifiers

PMID40682121
PMCPMC12506656

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.